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J Bacteriol. 1999 Oct; 181(20): 6223–6229.
PMCID: PMC103753

Opening the Iron Box: Transcriptional Metalloregulation by the Fur Protein

It is generally accepted that iron is the most important micronutrient used by bacteria. With members of the family Lactobacillae being the only exceptions so far (3), this metal is essential for cellular metabolism, since it is needed as a cofactor for a large number of enzymes (96). However, this element is not easily available to microorganisms in aerobic environments. While in anaerobic conditions Fe2+ is soluble at physiological pH and cells obtain iron without much difficulty from the external medium, the ion becomes quickly converted to Fe3+ upon exposure to oxygen and forms insoluble hydroxides at neutral pH, making the available metal very scarce (20). In order to acquire iron from the extracellular medium, virtually all aerobic bacteria produce and secrete low-molecular-weight compounds termed siderophores (sideros phoros, iron carriers). These compounds chelate Fe3+ with high affinity and specificity (68). Subsequently, the cell recovers the ferrisiderophore complexes through specific outer membrane receptors (30). Some of these high-affinity systems of iron uptake are important virulence factors in bacteria infecting animal fluids and tissues because they can chelate the metal bound to host proteins (7, 36, 60, 71). Furthermore, because iron availability is generally growth limiting for bacteria thriving in an animal millieu, the lack of the metal is a major environmental signal to trigger expression of virulence determinants (60). However, an excess of iron is toxic because of its ability to catalyse Fenton reactions and formation of active species of oxygen. Iron uptake has to be, therefore, exquisitely regulated to maintain the intracellular concentration of the metal between desirable limits. Considering that excretion mechanisms for iron are not known in bacteria, microorganisms appear to control iron homeostasis, regulating its transport through the membrane (5, 21).


A key breakthrough in the understanding of how bacteria regulate iron transport was the description by Hantke in 1981 (45) of an Escherichia coli mutant which behaved as if the expression of all known functions inhibited by iron (siderophore production and biosynthesis of distinct outer membrane proteins) were constitutively expressed. This mutant, which behaved like a Salmonella typhimurium mutant isolated sometime before (31), was named fur (for ferric uptake regulation), and its behavior clearly suggested that a metal-dependent repression was at the basis of the control exerted by iron on many, if not all, Fe-responsive genes. The fur gene was subsequently mapped (4), cloned (46), and sequenced (79), its protein product was purified (100), and some basic aspects of the regulation mechanism were elucidated (4, 45, 46).

The Fur protein of E. coli is a 17-kDa polypeptide (6, 78) which acts as a transcriptional repressor of iron-regulated promoters by virtue of its Fe2+-dependent DNA binding activity (5, 25, 32, 33). Figure Figure11 shows the long-accepted model of Fur-mediated repression of metalloregulated genes. Under iron-rich conditions Fur binds the divalent ion, acquires a configuration able to bind target DNA sequences (generally known as Fur boxes or iron boxes, Fig. Fig.2),2), and inhibits transcription from virtually all the genes and operons repressed by the metal. On the contrary, when iron is scarce, the equilibrium is displaced to release Fe2+, the RNA polymerase accesses cognate promoters, and the genes for the biosynthesis of siderophores and other iron-related functions are expressed (41, 55). In some cases (notably in Pseudomonas aeruginosa [58]) Fur may control expression of a sigma factor which, in turn, causes a discrete set of genes to be expressed. Homologues of the fur gene have been described for many Gram-negative bacteria, including several important human pathogens like Yersinia (82), Salmonella (31), Vibrio (59, 61, 90, 104), Pseudomonas (76, 95), Helicobacter pylori (8), Bordetella (14), Campylobacter (103), Acinetobacter baumannii (23), Legionella (51), Neisseria (9, 88, 89), and Haemophilus (17) and even for plant pathogens like Erwinia chrysanthemi (36). Fur-like proteins have been found also in Gram-positive bacteria, e.g., Bacillus subtilis (15) and Staphylococcus (49), and even in cyanobacteria (40). Most of these homologues are able to complement an E. coli fur mutant, suggesting that the molecular mechanisms that control transcriptional regulation by iron are shared by many microorganisms.

FIG. 1
Regulation of iron transport in E. coli. This classical model of response to iron starvation still remains basically correct (4). It is based on the existence of two configurations of the Fur protein in an equilibrium which is displaced by Fe2+ ...
FIG. 2
Alternative interpretations of the Fur box. The scheme shows different views of the 19-bp sequence bound by the repressor and generally known as the Fur box or the iron box in E. coli. The standard interpretation considers this box as a palindromic sequence ...

The Fur protein appears to be a dimer in solution regardless of the presence or absence of Fe2+ (19, 67, 69). On this basis, the protein has been proposed to have two different domains (19, 85). The C terminus is implicated in dimerization, whereas the N-terminal module accounts for the ability of the repressor to bind DNA (52, 85). Although several mutant alleles of fur have been described (12, 19, 43) and some protein variants have been purified, the constellation of amino acids that define the main metal binding site, as well as those implicated in dimerization or in interactions with DNA, remain to be elucidated. Furthermore, Fur is able to multimerize through protein-protein interactions (56), but the protein domains involved, perhaps different from those for dimerization, are unknown. In addition, Fur appears to be an abundant protein. Watnick et al. (98) found in Vibrio around 2,500 Fur molecules per cell during the logarithmic phase, which increased to 7,500 in the stationary stage. This relatively high amount of protein sharply contrasts with the generally low concentrations of other regulators. As discussed later, this might be connected not only to the large regulon controlled by the repressor but also to the unusual fashion with which this protein binds DNA (26, 34; see below).


In the last few years, the number of genes described as Fur-controlled have increased significantly for E. coli as well as for other bacteria (72, 84, 92). The large variety of genes controlled by this regulator has been revealed through the use of ingenious genetic and biochemical techniques. For instance, FURTA (Fur titration assays [84]), allow the detection of iron-regulated promoters from a cosmid or plasmid library. This method is based on the use of a chromosomal iron-regulated lacZ fusion to the fhuF gene. This fusion is exceptionally sensitive to small changes in iron concentration because of the weak affinity of the fhuF promoter for the Fur-Fe2+ repression complex. Introduction of a multicopy plasmid carrying Fur-binding sites into the test strain appears to deplete the intracellular Fur pool. This gives rise to the dissociation of the repressor from the fusion promoter, thereby allowing lacZ transcription. The screening of a plasmid gene bank from E. coli or S. typhimurium with this method led to the identification of numerous new Fur-controlled genes (84, 92; see below). On the other hand, the technique called SELEX (systematic evolution of ligands by exponential enrichment) has also been used successfully for isolating 16 novel Fur-dependent genes in P. aeruginosa (72). In this case, mixtures of chromosomal DNA fragments were passed through a filter bearing immobilized Fur protein, from which they were later extracted and amplified with the PCR. All newly found DNA sequences were protected by Fur in DNase I footprinting assays and, accordingly, were transcribed preferentially when cells faced iron starvation. In addition many of them bore similarity to siderophore receptors and alternative sigma factors (72).

An interesting counterpart of searching for iron-responsive promoters has been the identification of fur mutants in bacteria other than E. coli. In this respect, screening for manganese-resistant colonies has been a very effective method to pinpoint such mutants (47). This procedure is based on the observation that, at high concentrations, Mn2+ mimics Fe2+ and thus causes a lethal repression of the iron uptake systems (47). Cells that lack Fur escape such a repression and can thus be selected on plates. An overall picture of the complement of genes whose expression is affected by Fur in a given species can be drawn by comparing bidimensional protein electrophoresis patterns of the wild-type versus fur mutant variants. This approach has been successful in examining strains of various species such as Campylobacter jejuni (93), Vibrio cholerae (62), Yersinia pestis (83), Neisseria gonorrhoeae (89), and S. typhimurium (38). The combination of two-dimensional electrophoresis followed by reverse genetics for all these microorganisms has permitted identification of a large number of proteins and genes which are regulated or at least influenced by the Fur protein. More recently, the combined use of two-dimensional electrophoresis, mass spectrometry, and bioinformatic tools has allowed the identification of 10 iron-regulated proteins within the genome of Mycobacterium tuberculosis and their patterns of expression (102).

Inspection of the genes found to be regulated by Fur has revealed that this protein participates also in functions not directly related to iron metabolism. These include cellular processes as varied as the acid shock response (43), defense against oxygen radicals (70, 87), chemotaxis (54), metabolic pathways (47, 84), bioluminescence (65), swarming (66), and production of toxins and other virulence factors (60). In fact, as mentioned above, coupling expression of virulence factors to iron starvation makes sense given the lack of available metal that is predominant in host fluids and tissues. This seems to be the case for Shiga toxin in Shigella (60) for Shiga-like toxin I (60) and colicin V and hemolysin (37) in E. coli, and for exotoxin A in P. aeruginosa (76, 94). The same applies to the observed inhibition by iron of fimbrial expression in enterotoxigenic E. coli (54) and the involvement of Fur in virulence of plant pathogens such as E. chrysanthemi (36).

In other cases, the meaning of the iron regulation of some genes is more obscure. For instance, Fur appears to control flagellum assembly and chemotaxis through the regulation of one of its main transcriptional activators, FlhD (positive in the FURTA assay [84]). In this case, Fur seems to couple iron status to motility, so that expression of the flagella is inhibited when bacteria have an excess of the metal. This may prevent the departure of the cells towards other environments with less available iron (66, 84). Along the line, Fur-mediated repression of key metabolic genes such as purR or metJ (again positives in the FURTA assay [84]) might help the fine-tuning of cell metabolism for optimal growth conditions. Fur also represses some genes induced in response to oxidative stress like the Mn-dependent superoxide dismutase (MnSOD) gene, sodA, in E. coli (87) and P. aeruginosa (48) or the 8-hydroxyguanine endonuclease gene in E. coli (57). Since MnSOD is a key enzyme in defense against oxygen toxicity, the physiological significance of this negative regulation is unclear. Given that an excess of iron may lead to Fenton chemistry reactions and thus to oxidative stress, perhaps expression of MnSOD along with siderophore production prevents the damaging effects of a transient iron overload (91).

While these functions are not directly related to iron transport they can at least be understood mechanistically, considering Fur as a transcriptional repressor. However, a few intriguing cases have been reported in recent years in which Fur appears to act positively rather than negatively in the expression of certain promoters. The most remarkable instance is the expression of the acid tolerance response of S. typhimurium. This phenomenon requires Fur, the absence of which prevents expression of key acid shock proteins (43). The acid-sensing and the iron-sensing mechanisms mediated by Fur in this microorganism can be separated by mutations in the protein. A change in the H90 residue of the repressor makes Fur blind to iron (i.e., it becomes unable to repress cognate promoters), while it still maintains its function as mediator of the acid shock response (43). The proteins which act as indicators of such a response belong to the group of at least 34 polypeptides of S. typhimurium whose expression is affected by the loss of the Fur product (38). The existence of positively regulated genes in the E. coli Fur regulon has been also suggested (47, 70). The observation that the fur mutant grew poorly on succinate suggested that the protein activates the uptake and/or the catabolism of this carbon source (47). In addition, it has been proposed that expression of sodB, encoding an Fe-dependent superoxide dismutase (FeSOD), is controlled positively by Fur (70). Moreover, fur mutants have low levels of several iron-containing proteins such as fumarases A and B and aconitase A, thus raising the possibility that Fur is implicated in more activities involving iron metabolism in the cell (1). On the other hand, the operons for bacterioferritins (brfA-katA [64]) and catalase/peroxidase (brfB-aphA [73]) in P. aeruginosa are expressed in response to oxidative stress and to the presence of iron. Although cases where given genes or given products (38, 62, 83, 89, 93, 102) appear to be activated rather than repressed by Fur, the hard fact is that the function of the protein as a transcriptional activator has never been rigorously proven. Direct interactions between the Fur protein and the promoter regions of the iron-activated genes have never been shown. Therefore, so far Fur appears to be exclusively a repressor and its positive effects on certain promoters are likely to be the result of indirect rather than direct effects.

That Fur could have different roles in distinct species has been suggested by the observation that the gene is essential in Neisseria (9, 88), Pseudomonas (76, 95), Rhizobium (28), and Vibrio anguillarum (90) but not in E. coli (45), Bacillus (15), Yersinia (82), or Vibrio cholerae (62). On the other hand, the abundance of promoters that are regulated one way or another by this protein is reminiscent of the effects of global regulators such as Fis, integration host factor, HU, Lrp and H-NS, as has been already proposed for the Fur protein of V. anguillarum (18). These proteins control directly the output of only a few specific promoters, while they exert a direct or indirect effect on the performance of many others. Since iron influences so many processes in the cell, it is tempting to also consider Fur more like a global regulator which adjusts the entire metabolism to changes in environmental iron than like a very specific transcription factor for a few siderophore promoters. Being a general regulator, however, requires that binding sites are not limited to very specific sequences but can also be used for more relaxed and abundant DNA targets. How does this fit with what we know about the interactions of Fur with the promoters of metalloregulated genes?


As soon as Fur became available as a purified protein (100) it became possible to study in vitro the interaction between Fur-Fe2+ and a few iron-responsive promoters of E. coli (13, 25, 27, 42, 53, 87). The DNase I analyses of several Fur-binding sites allowed the early definition of a 19-bp consensus Fur box (i.e., the iron box; Fig. Fig.2).2). Additional in vivo assays showed that this sequence, cloned downstream of a heterologous promoter, was sufficient to ensure that its transcriptional activity was regulated by iron (16). At a later point, sequence alignment of a collection of more than 30 iron-controlled promoters of various origins (12) confirmed that the sequence 5′GATAATGATAATCATTATC3′ was the functional target of the Fur protein. This, together with the apparent dimeric nature of the protein (19, 67, 69), suggested a mode of Fur-DNA interaction similar to that of classical bacterial repressors, in which a protein dimer recognizes a palindromic DNA sequence (77). But other results are not compatible with this notion. Hydroxyl radical footprinting of Fur within the promoter of the aerobactin (siderophore) operon (10, 24), revealed that protein binding to its target site gives rise to a distinct pattern of two protected and four nonprotected base pairs which is repeated three times along the primary binding site (26). On the other hand, many iron-regulated promoters appear to have not just one Fur box but multiple, sometimes overlapping, boxes (42, 53, 87), which is hardly compatible with the dimer-palindrome model (77). Furthermore, it appears that Fur wraps helically around the DNA, as indicated not only by the hydroxyl radical data (26) but also by direct electron microscopy observations (37, 56). How can all these observations be reconciled?

As shown in Fig. Fig.2,2, the iron box motif can be interpreted as a palindrome formed by two 9-bp inverted repeats, 5′GATAATGAT3′, separated by one unmatched A. But interestingly, the same 19-bp sequence can be viewed as a combination of three adjacent repeats, 5′NATA/TAT3′. Since the pattern of Fur-DNA interaction revealed by hydroxyl radical footprinting of the aerobactin promoter (26) consists of a succession of equivalent protections with a periodicity of 6 bp, it became plausible that the consensus sequence could in fact be recognized by Fur as three repeats of 6 bp rather than as a 19-bp palindrome. A recent study suggests that this could in fact be the case (34). We have observed that while a minimum of three repeats is required to produce an effective Fur binding site, their relative orientation and their number may not be so important. The hexamer NATA/TAT appears to be the unit of interaction with Fur in a target site, although only the sum of DNA-protein and protein-protein interactions involving at least three units may endow the complex with enough strength and specificity to be fully functional (34; Fig. Fig.3).3).

FIG. 3
Rules that govern the generation of Fur binding sites. Active targets for the Fur-Fe2+ complex can be assembled by combining a minimum of three repeats of NATA/TAT. (A) The thymines present in the core sequence AT-AT of each repeat are directly ...

These notions about the true nature of Fur boxes as an array of shorter sequence motifs could explain why the target DNA admits so many changes and why no individual bases essential for the interaction have been found in mutagenesis experiments (84). Fur-DNA interaction may therefore be quite different from the classical model of LacI, Cro, or catabolite gene activator protein, in which a dimeric (or tetrameric) protein binds a palindromic sequence (77). This type of interaction could provide the protein with the ability to behave both as a very specific repressor and as a more general regulator.


As mentioned above, fur gene homologues have been found in a variety of gram-negative species. Since the cognate protein sequences exhibit a high degree of similarity, it is predictable that very closely related target sequences will also be found at iron-regulated promoters in microorganisms such as members of the family Enterobacteriaceae. In fact, this is the case in every single instance where the issue has been examined. Bacteria bearing Fur homologues systematically also possess Fur boxes in front of the fur gene or other iron-regulated genes (29, 35, 51, 88). In many cases, binding of such sequences by FurEC (the Fur protein from E. coli) has been observed in in vitro or in vivo assays. For instance, some Pseudomonas genes that are regulated by Fur are retarded in band-shift gels and protected in footprinting assays with the protein from E. coli (71, 74). Similarly, the fbpA gene of N. gonorrhoeae (encoding a periplasmic binding protein) is both regulated by FurEC in in vivo and protected from DNase I in vitro (9, 29). In vivo FURTA assays using E. coli as a host have highlighted the efficiency of DNA sequences of various origins in binding FurEC. These include the promoter regions of the pfrI and pupIR genes from Pseudomonas putida (95), the sfuA gene of Serratia marcescens, and the genes hemPR (heme uptake operon) and foxA/fcuA (extracellular ferrioxamin receptor) from Yersinia enterocolitica (84). But this is not limited to gram-negative bacteria. The genome of B. subtilis also contains perfect Fur boxes in the promoter regions of siderophore-related genes (15) whose functionality in binding FurEC in vivo has been proved in some cases (81). The recognition of the consensus Fur box of E. coli by the Fur protein of B. subtilis is consistent with the similarity of the DNA binding motifs of both repressors (15).

But what about interactions of Fur homologues with DNA sequences in their cognate hosts? Although the data is more scarce than for E. coli, the few instances where the issue has been examined do indicate that all Fur proteins bind the same consensus target DNA. Canonical iron boxes bind the Fur products of C. jejuni (63), P. aeruginosa (48, 58), Vibrio anguillarum (18), and V. cholerae (99), as revealed with in vitro band-shift assays. Furthermore, DNase I footprinting experiments of FurPA with a large collection of P. aeruginosa DNA fragments selected with SELEX have revealed that the general organization of the Fur boxes and the protected sequences in this microorganism are virtually identical to those described for E. coli (48, 72). The promoters examined contained one or two overlapping or tandemly organized Fur binding motifs with a consensus identical to that of E. coli. In addition, the protected sequences added up to the standard 30 to 38 bp protected by the protein which have been repeatedly observed in Fur sites of E. coli promoters. Likewise, the characterization of the interaction between Fur and the promoter of the iron transport fatDCBA operon in V. anguillarum has revealed several complexes in gel retardation assays and extended protected sequences in DNase I gels (18). This promoter is AT rich, but not all portions of the binding sequences showed a clear conservation of the consensus Fur box or the characteristic dyad symmetry. This is not unlike what has been described for the Fur polymerization region in the aerobactin promoter (25, 26). Most sequences of P. aeruginosa, V. anguillarum, and other bacteria targeted by their native Fur proteins could be reinterpreted as arrays of NATA/TAT sequences, as discussed above. The generalization of this concept requires, however, further investigation.

Although B. subtilis and Staphylococcus aureus do possess a distinct Fur-like homologue (15, 49), the protein known as the diphtheria toxin regulator (DtxR) of Corynebacterium diphtheriae constitutes the archetype of a class of iron-related regulators found in gram-positive bacteria (11). This class includes SirR of Staphylococcus epidermidis (50) and IdeR of M. tuberculosis (80). DtxR does not have much similarity to Fur (less than 20% identity at the amino acid level), and complementation between these proteins is weak or nonexistent (11). The crystal structure of DtxR has revealed that two dimeric repressor proteins are bound to opposite sides of the tox operator (101). Although the operator sequences bound by DtxR bear some similarity to the Fur box and the primary region protected from DNase I also spans 30 bp, it is plausible that DtxR and Fur have different DNA binding mechanisms (86, 97).


The type of regulation described for Fur may also be applicable to other metal-dependent repressors. In this respect, the Zur (zinc uptake regulator) protein, described thus far in E. coli (75), B. subtilis (39), and Listeria monocytogenes (22), is worth a comment. Similar to iron, Zn is an element that, depending on the concentration, can be an essential micronutrient or a potent toxin. The uptake of this metal is regulated by the Zur protein in combination with zinc, resembling the phenomenology already discussed for Fur. Furthermore, Zur and Fur have a significant sequence identity (24% in B. subtilis and 27% in E. coli [39, 75]). Nothing is known about the repression mechanism, but some Zur-binding sequences have been described for promoters of genes related to Zn uptake, and, intriguingly, they are similar to the Fur box (39). This may allow a degree of regulatory cross-talk but must also permit each repressor to recognize and regulate specifically their own set of genes. It will be interesting to analyze whether Zur uses the same molecular mechanisms as Fur to repress transcription and bind DNA. Some proteins initially found through genomic search and classified as Fur homologues are certainly more similar to Zur than to Fur (75) and perhaps could be reclassified as regulators of zinc uptake. Moreover, the fact that Fur has been recently defined as a Zn-metalloprotein containing one structural ion of Zn2+ per polypeptide makes the relation between these proteins even more complex (2).

Analysis of the growing number of the genomes of bacterial species which have been or are being completely sequenced, as well as direct experimental observations, have started to unveil the existence of an entire family proteins structurally related to Fur which control gene expression in response to different stress signals. Besides Fur and Zur, B. subtilis harbors one more related protein called PerR (15). The PerR regulon includes genes involved in the response to oxidative stress such as katA (encoding catalase A) and aphC (alkyl hydroperoxide reductase) as well as fur and perR. Although these genes can be repressed by either manganese or iron, the PerR-Fe2+ complex is the form that reacts with hydrogen peroxide to cause derepression (15). The Per boxes are thus associated with oxidative stress genes in several gram-positive bacteria rather than with iron transport. The Irr product of Bradyrhizobium japonicum also bears a considerable similarity (29% identity [44]) to the Fur protein of E. coli. The Irr protein regulates heme biosynthesis and appears to coordinate this pathway with iron homeostasis (which is in itself regulated by a genuine Fur homologue in this bacterium). In contrast to Fur, Irr is active under iron limitation. As in the case of Zur, some proteins described as Fur homologues could functionally be Irr-like regulators (44).


The abundance of the protein, the form of interaction with target DNA sequences, and the involvement of Fur in many cell functions indicate that this protein performs more like a general regulator than as a specific repressor. The reinterpretation of Fur binding sites with the NATA/TAT array model affords not only an explanation of many thus far unaccounted for results about the interaction of the protein with its target sequences but also provides a basis for understanding the differences observed in the responses of various genes to physiological iron status. The combination of repetitive sequence elements that allow cooperative binding of the Fur protein in extended promoter regions would explain how a relatively simple protein controls a complex regulon in a gradual fashion. The intracellular iron concentration and the variability and extension of the sequences targeted by the protein may cause an ample range of responses in each specific case. On this basis, some genes like fur undergo mild regulation or coregulation by iron, while others like the aerobactin operon in E. coli are subject to a strong repression/induction switch.


The work of this Laboratory on metalloregulation is funded by grants ENV4-CT95-0141 (Environment) of the EU and grant BIO98-0808 of the Comisión Interministerial de Ciencia y Tecnología.

We are indebted to J. B. Neilands for constant inspiration of work on iron metabolism in microorganisms.


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